ClinVar Miner

Submissions for variant NM_032856.5(WDR73):c.293T>C (p.Leu98Pro)

dbSNP: rs863223396
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Human Genetics Laboratory, Faculty of Medicine of Tunis RCV000785981 SCV000924323 likely pathogenic Galloway-Mowat syndrome 1 2018-10-10 no assertion criteria provided case-control

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